INSIGHTS Registry: Inspiring New Science in Guiding Healthcare in Turner syndrome

INSIGHTS REGISTRY - Inspiring New Science in Guiding Healthcare in Turner syndrome logo and TSGA - Turner syndrome global alliance logo

Purpose of the study: INSIGHTS is a registry study that  collects  key  information  on  medical history  for  girls  and  women  with  Turner  syndrome  and  the  clinical  care  they receive. This includes genetic tests, imaging, medications, and more for hundreds of patients seen at a number of clinics across the US. In addition to learning a lot about the current state of health for individuals with TS, INSIGHTS serves as an infrastructure  to  conduct  future  studies  that  are  meaningful  to  patients  and  their families.

What’s Involved: Patients who enroll in the INSIGHTS registry give permission to use their medical records for research purposes. They can also choose to be included on recruitment list  for  future  studies,  participate  in  some  surveys  about  themselves,  and  allow researchers to save their blood  to use for future research. This information gets stored  in  a  secure  database.  De-identified information can then be given to researchers approved by the Steering Committee. The Steering Committee will only approve proposals that will provide meaningful knowledge to the TS community.  

To learn more about this study, contact 720-777-0705 or email insights@ucdenver.edu.
(COMIRB# 19-3027, ; PI Dr. Shanlee Davis; funded by TSGA)

You can also enroll yourself/your child in the registry online without coming into clinic, .

with up-to-date enrollment and demographic data on INSIGHTS participants!

Turner syndrome global alliance logo

INSIGHTS results have been presented at academic conferences:

2024

Annual Clinical Genetics Meeting

Natalia Klamut, a research coordinator, had a poster about Turner syndrome mosaicism with Trisomy X. We found that mosaicism with a Trisomy X cell line may be more common than reported before. We identified differences between non-mosaic individuals and mosaic with Trisomy X individuals. (For example, we found more structure heart disease, aortic concerns, and short stature in the non-mosaic group than the mosaic with Trisomy X group.) We also identified difference between mosaic with Trisomy X individuals and mosaic with 46,XX individuals. (For example, we found than mosaic with Trisomy X individuals were more likely to have neurodevelopmental concerns than mosaic with 46,XX individuals.) Previous research has not reported this difference. The Trisomy X cell line may have unique contributions that affect counseling and clinical care.

  • See her abstract here: .
  • .

Megan Bettencourt, a genetic counseling student, presented on the prevalence of autism spectrum disorders (ASD) in individuals with Turner syndrome. She found that 12% of her participants had an ASD diagnosis, which was higher than expected. Behavioral disorder and global developmental delay had significant relationships with ASD. This is not different than the general population. We did not find any different or new predictors of an ASD diagnosis in Turner syndrome. Since the prevalence of ASD was high, the results support screening for ASD in children with Turner syndrome. 

  • See her abstract here: .
  • .


2022

Western Society for Pediatric Research

Dr. Shanlee Davis presented an abstract about the diversity of the sample in INSIGHTS. Over 18% of the sample identified as Hispanic/Latinx and about 28% of the sample identified as non-white. Stakeholder engagement in the development of the registry helped successfully recruit a diverse sample. 

 

Pediatric Endocrine Society Annual Meeting

Alexandra Carl, MPH presented an abstract about the demographics of the sample in the INSIGHTS Registry and describing the timing of the Turner syndrome diagnosis. About 14% of participants were diagnosed with Turner syndrome (TS) due to incidental screening. TS patients diagnosed incidentally did not differ from those that are diagnosed secondary to symptoms in terms of karyotype or demographic characteristics. Incidentally identified patients were more likely to be diagnosed prenatally, which was expected due to the use of non-invasive prenatal testing (NIPT).

 

Natalia Klamut, an undergraduate research assistant, presented an abstract about Turner syndrome mosaicism with a Trisomy X (XXX) cell line. Individuals with trisomy X mosaicism were more likely to be diagnosed at an older age than non-mosaic individuals. Those with trisomy X mosaicism were also more likely to be diagnosed secondary to delayed puberty/amenorrhea and short stature and less likely to be diagnosed secondary to dysmorphic features or congenital anomaly than those with non-mosaic TS.

INSIGHTS Steering Committee

Steering Committee Members:

  • - pediatric endocrinologist, Medical Director of the Growth Center, and Director of the Turner Syndrome Program at Children's Hospital of Philadelphia
  • - pediatric endocrinology and lead of the Turner Syndrome Clinic at Ann & Robert H Lurie Children's Hospital of Chicago
  • - medical geneticist at Johns Hopkins All Children's Hospital 
  • - pediatric endocrinologist and director of the Turner Syndrome Clinic at the Children's Hospital 麻豆传媒高清/University of 麻豆传媒高清
  • - division director of gynecology at Children's Mercy Hospital 
  • - founder and program coordinator of Turner Syndrome Global Alliance
  • - genetic counselor at the Children's Hospital 麻豆传媒高清/University of 麻豆传媒高清
  • - pediatric endocrinologist at Nationwide Children's Hospital 
  • - pediatric endocrinologist and Medical Director of the Turner Syndrome Clinic at the University of North Carolina
  • - cardiologist at the University of Texas Houston Medical Center
  • - founder and president of Turner Syndrome Global Alliance
  • pediatric endocrinology and lead of the Turner Syndrome Clinic at Children's National Hospital
  • - research psychologist at the University of 麻豆传媒高清

Important Documents:

 

Department of Pediatrics

CU Anschutz

Administrative Pavilion

13123 E. 16th Ave.

B065

Aurora, CO 80045


720-777-2715

 

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